Lead Analyst - Real Word Data - Pharma

Job Requirement:

- Innovation - Process Efficiency, Creative Thinking, Problem Solving and Decision Making, Scientific Leadership and Strategy, Negotiation Skills, strategic thinking

- Performance - Technical Expertise (Programming with SAS/R), RWD Knowledge, RWD Analytics, Data Interpretation and scientific support, Therapy area/asset knowledge, Epidemiological concepts, Scientific document comprehension, Industry Knowledge/Competitive Intelligence, Technical and Business Communication, Quality and Governance, QC skills, IT skills, consulting, project management

Key Responsibilities:

- Proactively identify issues and gaps in existing processes with minimal supervision and make the processes efficient with help of technology (SAS/R/Python codes, dashboards) so that the results obtained are of high quality in quicker turnaround time; Develops algorithms for repetitive processes; may use advanced technology

- Identifies and implements various ways that add more value to an already existing study/new study in terms of data interpretation and research methodology

- Works on RDQs, protocols, feasibility studies etc. using their expertise in SAS/R programming and databases; anticipates problems related to assigned work or areas of expertise and able to implement solutions, proactively seeking input from colleagues as needed; makes independent study related decisions, consults project programmer as needed

- Negotiates the project timelines, iterations, feasible study methodology and expectations independently which is agreeable by stakeholder

- Creates documents like data dictionary, business rules for various datasets, should know RWD connected to respective therapeutic area, guides and trains the team

- Has good knowledge on various therapy areas and epidemiological concepts to perform a sense check of the outputs of RDQs and protocol studies, applies their therapy area knowledge to give insightful information to the RWA team member supporting the output of the RDQ/protocol studies

- Applies, guides, and ensures others in team are following standard processes on tasks, ensuring that deliverables are accurate and within timelines

- Has strong knowledge of Good Practice (GxP), International Council for Harmonisation (ICH) requirements, internal processes and external regulations that govern drug development (wherever applicable)

- Acts as an auditor for the team to make sure the team adheres to the defined quality standards

- Adheres to the technical plan for a project execution, learns and adapts to the best technology to be leveraged in a project, mentors the team in data interpretation and analysis

- Communicates effectively and precisely on regular projects updates, flags risks proactively, negotiates on reasonable timelines, presents study outcomes and insights

- Understands and Quickly adapts to the change in scope of day to day work and guides team members to adapt to the new change

- Is a reliable trusted knowledge partner to stakeholders, acts as a single point of contact for stakeholder for their study related needs

- Must embrace and be compliant to the defined culture

- Should take accountability of their regular work and secondary QC work

- Assists the managers by providing constructive feedback on strengths and area of improvements of members mentored, assists in recruitment process to hire best talent in RWD